Interaction Of Cations Research Articles

CO2 absorption using two morpholine protic ionic liquids: measurement, model, and quantum chemical calculation

Two kinds of protic ionic liquids, N-methylmorpholinium formate ([NMMH][For]) and N-ethylmorpholinium formate ([NEMH][For]), were synthesized by the acid-base neutralization method. The solubility of carbon dioxide (CO2) in the two ionic liquids was measured at temperatures of 298.15 to 338.15 K and pressures of up to 900 kPa. The solubility increases linearly with pressure, indicating that CO2 is physically absorbed in ionic liquids. The solubility of CO2 in [NEMH][For] is higher than that of [NMMH][For]. Absorption behavior was investigated by thermodynamic properties, such as the Henry's law constant, partial molar Gibbs free energy, partial molar enthalpy, and partial molar entropy. The Pitzer's model and the Soave-Redlich-Kwong (SRK) cubic equation of state were used to fit the solubility data, respectively. The Pitzer's model is found to have better prediction accuracy. The interaction of two protic ionic liquids with CO2 was analyzed using quantum chemistry. The molecular mechanism of CO2 absorption by two protic ionic liquids was explained from the microscopic point of view. CO2 + [NEMH][For] has more hydrogen bonds and a higher interaction energy. The cation–anion interaction of [NEMH][For] diminishes in the presence of CO2, resulting in an increase in the cation–anion distance. These factors result in higher solubility of CO2 in [NEMH][For].

Multiscale modeling of CO2 capture in dicationic ionic liquids: Evaluating the influence of hydroxyl groups using DFT-IR, COSMO-RS, and MD simulation methods.

This work employs a combination of density functional theory-infrared (IR), conductor-like screening model for real solvents (COSMO-RS), and molecular dynamic (MD) methods to investigate the impact of hydroxyl functional groups on CO2 capture within dicationic ionic liquids (DILs). The COSMO-RS reveals that hydroxyl groups in DILs reduce the macroscopic solubility of CO2 but improve the selectivity of CO2 over CO, H2, and CH4 gases. Quantum methods in the gas phase and MD simulations in the liquid phase were conducted to delve deeper into the underlying mechanisms. The IR spectrum analysis confirms red shifts in CO2's asymmetric stretching mode and blue shifts in the CR-HR bond of the dication, indicating CO2-DIL interactions and the weakening of the anion-cation interactions caused by the presence of CO2. The results show that the positioning of anions around hydroxyl groups and HR atoms in rings inhibits the proximity of CO2 molecules, causing the hydrogen atoms within methylene groups to accumulate CO2. van der Waals forces were found to dominate the interaction between ions and CO2. The addition of hydroxyl groups strengthens the electrostatic interactions and hydrogen bonds between dications and anions. The stronger interaction energy between ions in [C5(mim)2-(C2)2(OH)2][NTf2]2 limits the displacement of CO2 molecules within this DIL compared to [C5(mim)2-(C4)2][NTf2]2. Compared to [C5(mim)2-(C4)2][NTf2]2, [C5(mim)2-(C2)2(OH)2][NTf2]2 exhibits stronger ion-ion interactions, higher density, and reduced free volume, resulting in a reduction in CO2 capture. These results provide significant insights into the intermolecular interactions and vibrational properties of CO2 in DIL complexes, emphasizing their significance in developing efficient and sustainable strategies for CO2 capture.

Current analysis of cations substitution in the oxygen-evolving complex of photosystem II.

Water oxidation in photosystem II (PSII) is performed by the oxygen-evolving complex Mn4CaO5 which can be extracted from PSII and then reconstructed using exogenous cations Mn(II) and Ca2+. The binding efficiency of other cations to the Mn-binding sites in Mn-depleted PSII was investigated without any positive results. At the same time, a study of the Fe cations interaction with Mn-binding sites showed that it binds at a level comparable with the binding of Mn cations. Binding of Fe(II) cations first requires its light-dependent oxidation. In general, the interaction of Fe(II) with Mn-depleted PSII has a number of features similar to the two-quantum model of photoactivation of the complex with the release of oxygen. Interestingly, incubation of Ca-depleted PSII with Fe(II) cations under certain conditions is accompanied by the formation of a chimeric cluster Mn/Fe in the oxygen-evolving complex. PSII with the cluster 2Mn2Fe was found to be capable of water oxidation, but only to the H2O2 intermediate. However, the cluster 3Mn1Fe can oxidize water to O2 with an efficiency about 25% of the original in the absence of extrinsic proteins PsbQ and PsbP. In the presence of these proteins, the efficiency of O2 evolution can reach 80% of the original when adding exogenous Ca2+. In this review, we summarized information on the formation of chimeric Mn-Fe clusters in the oxygen-evolving complex. The data cited may be useful for detailing the mechanism of water oxidation.

Releasing Free Anions by High Donor Number Cosolvent in Noncorrosive Electrolytes of Commercially Available Magnesium Salts.

Passivation of the magnesium (Mg) anode in the chloride-free electrolytes using commercially available Mg salts is a critical issue for rechargeable Mg batteries. Herein, a high donor number cosolvent of 1-methylimidazolium (MeIm) is introduced into Mg(TFSI)2- and Mg(HMDS)2-based electrolytes to address the passivation problem and realize highly reversible Mg plating/stripping. Theoretical calculations and experimental characterization results reveal that the strong coordination ability of MeIm with Mg2+ can weaken the anion-cation interactions and promote the formation of free anions that have higher reduction stability, thus significantly suppressing anion-derived passivation layer formation. By adding MeIm cosolvent into Mg(TFSI)2-based electrolyte, the average Coulombic efficiency of the Mg//Cu cell is increased from less than 20% to over 90%, and the Mg//Mg cell can stably cycle for over 800 h with a low overpotential. In the MeIm-regulated Mg(HMDS)2-based electrolyte, the solvation structure change, featured by an effective separation of Mg2+ and HMDS-, greatly increases the ionic conductivity by more than 30 times. This solvation structure regulation strategy for noncorrosive electrolytes of commercially available Mg salts has a great potential for application in future rechargeable Mg metal batteries.

Effect of ionic association on the pressure-driven Li+/Mg2+ permselective transport through nanochannels

It is extremely significant to develop lithium recovery technology due to the growing consumption of the lithium in the past few years. Membrane separation offers a green process for lithium recovery, however, there are still some debates on its mechanism. Ionic association is a common behavior among the cation–anion interaction in the aqueous solution, which is believed to take effect on the ionic permeation through the available membranes. In this work, a series of MD simulations were performed to unravel the effect of ionic association on the Li+/Mg2+ permselective transport through one-dimensional nanochannels, which were modelled for mimicking the channels with the interested sizes of the commonly-used membranes rather than any specific membranes. Two types of structural evolutions (i.e. dehydration and disassociation) were found during the penetration of the ionic associations into the nanochannels, the ionic associations significantly impede the ionic transmembrane permeation. The electrostatic affinity of the cations determines the structure of the ionic associations. As a result, the divalent Mg2+ ions lead to a preferred formation of hyper-associations, which makes the Mg2+ associations have to enter into the nanochannel via disassociation. While it is relatively easy for the Li+ associations to squeeze into the confinement via disassociation or dehydration, and even some free Li+ ions could penetrate into the nanochannels. However, the coexistence of the Li+ and Mg2+ ions greatly deteriorates the preferential permeation to Li+ ions due to the enhance ionic association, which thus greatly reduces the Li+/Mg2+ permselectivity. Therefore, it is of significant importance to disorganize the ionic association structures of the Li+ and Mg2+ ions in order to achieve a precise size-sieving capacity of nanochannels for efficient Li+/Mg2+ separation. This work not only helps understand the effect of association on membrane-based Li+/Mg2+ separation, but also promotes the development of high-performance membranes for Li+/Mg2+ separation.

The electrochemistry of stable sulfur isotopes versus lithium

Sulfur in nature consists of two abundant stable isotopes, with two more neutrons in the heavy one (34S) than in the light one (32S). The two isotopes show similar physicochemical properties and are usually considered an integral system for chemical research in various fields. In this work, a model study based on a Li-S battery was performed to reveal the variation between the electrochemical properties of the two S isotopes. Provided with the same octatomic ring structure, the cyclo-34S8 molecules form stronger S-S bonds than cyclo-32S8 and are more prone to react with Li. The soluble Li polysulfides generated by the Li-34S conversion reaction show a stronger cation-solvent interaction yet a weaker cation-anion interaction than the 32S-based counterparts, which facilitates quick solvation of polysulfides yet hinders their migration from the cathode to the anode. Consequently, the Li-34S cell shows improved cathode reaction kinetics at the solid-liquid interface and inhibited shuttle of polysulfides through the electrolyte so that it demonstrates better cycling performance than the Li-32S cell. Based on the varied shuttle kinetics of the isotopic-S-based polysulfides, an electrochemical separation method for 34S/32S isotope is proposed, which enables a notably higher separation factor than the conventional separation methods via chemical exchange or distillation and brings opportunities to low-cost manufacture, utilization, and research of heavy chalcogen isotopes.

Liquid Structure of Ionic Liquids with [NTf2]- Anions, Derived from Neutron Scattering.

The liquid structure of three common ionic liquids (ILs) was investigated by neutron scattering for the first time. The ILs were based on the bis(trifluoromethanesulfonyl)imide anion, abbreviated in the literature as [NTf2]- or [TFSI]-, and on the following cations: 1-ethyl-3-methylimidazolium, [C2mim]+; 1-decyl-3-methylimidazolium, [C10mim]+; and trihexyl(tetradecyl)phosphonium, [P666,14]+. Comparative analysis of the three ILs confirmed increased size of nonpolar nanodomains with increasing bulk of alkyl chains. It also sheds light on the cation-anion interactions, providing experimental insight into strength, directionality, and angle of hydrogen bonds between protons on the imidazolium ring, as well as H-C-P protons in [P666,14]+, to oxygen and nitrogen atoms in the [NTf2]-. The new Dissolve data analysis package enabled, for the first time, the analysis of neutron scattering data of ILs with long alkyl chains, in particular, of [P666,14][NTf2]. Results generated with Dissolve were validated by comparing outputs from three different models, starting from three different sets of cation charges, for each of the three ILs, which gave convergent outcomes. Finally, a modified method for the synthesis of perdeuterated [P666,14][NTf2] has been reported, with the aim of reporting a complete set of synthetic and data processing approaches, laying robust foundations that enable the study of the phosphonium ILs family by neutron scattering.

Effect of Monovalent Cations on the Structure and Dynamics of Multimodal Chromatographic Surfaces.

While multimodal (MM) chromatography is a promising approach for purifying proteins, the lack of a fundamental understanding of how ion-ligand interactions govern selectivity limits its use in the biopharmaceutical industry. This study uses molecular dynamics simulations to study the interactions between simple monovalent cations and two commonly used structurally similar multimodal chromatography ligands, the Capto ligand and Nuvia cPrime, immobilized on the surface. On the Capto ligand surface, ion presence and type play a key role in modulating the formation of phenyl rings and carboxylate clusters. The flexible linkage attaching the Capto ligand to the self-assembled monolayer (SAM) surface allowed multiple ligands to form interactions with the small cations, while large cations interacted less strongly, following the order Li+ > Na+ > K+ > Cs+. Thus, smaller cations resulted in greater ordering on the surface and lower ion diffusivities, while larger cations resulted in less ordering and higher ion diffusivities, following the order Li+ < Na+ < K+ < Cs+. In contrast, due to the rigid attachment of Nuvia cPrime to the SAM surfaces, the cations bound less strongly and had a much smaller effect on ligand clustering or ordering. Additionally, ions in the presence of the Nuvia cPrime surface had generally greater diffusivities than those in the presence of the Capto ligand. Overall, the interaction of cations with the multimodal ligands can lead to unique configurations on the SAM that likely contribute to differential behavior in biological separations.

Synergistic adsorption removal of heavy metal oxoanions and cations from aqueous solution by a polyacrylate-coated ferrous sulfide and layered double hydroxide nanocomposite

Heavy metal oxoanions and cations often co-exist in the environment and it is a critical challenge to achieve their simultaneous and efficient removal due to their presence of opposite charges. Here, a polyacrylate-coated ferrous sulfide and layered double hydroxide (PAA/FeS@LDH) nanocomposite was developed. Results illustrated that PAA/FeS@LDH exhibited excellent reductivity and stability due to the dispersion of PAA and the support by LDH. The removal efficiency of single Cr(VI) (9.73 mg/L) using PAA/FeS@LDH reached 100 % within 120 min, which was significantly higher than that of LDH (35.39 %), FeS (73.13 %), and FeS/LDH (96.47 %). Attractively, an enhanced removal of Cr(VI) (19.46 mg/L) by PAA/FeS@LDH in the presence of Cu(II), Ni(II), or Cd(II) was observed, with Cr(VI) removal efficiency increasing from 49.63 % (single Cr(VI)) to 99.51 %, 82.46 %, and 72.18 % within 30 min, respectively. The adsorption capacities of Cr(VI) significantly enlarged from 140 mg Cr/g (single Cr(VI)) to 221, 175, and 171 mg Cr/g when co-existing with Cu(II), Ni(II), or Cd(II), respectively. Another interesting outcome was the significant enhancement of reusability of PAA/FeS@LDH by the co-existence of Cr(VI) and Cu(II). After 5 cycles, PAA/FeS@LDH could still remove 96.97 % of Cr(VI) together with >70 % of Cu(II) in the mixed solution, by contrast, the removal efficiency of Cr(VI) was only 38.04 % in a single solution. The characterization analysis and density functional theory calculations demonstrated that besides surface reduction, complexation and precipitation, the cation-anion bridge interaction was an essential mechanism of achieving the synergistic removal of heavy metal oxoanions and cations.

Microplastics affect membrane biofouling and microbial communities during gravity-driven membrane filtration of primary wastewater

Recently, gravity-driven membrane (GDM) filtration has been adopted as an alternative solution for decentralized wastewater treatment due to easy installation and maintenance, reduced energy and operation cost, and low global warming impact. This study investigated the influence of microplastic size (0.5–0.8 μm and 40–48 μm) and amount (0.1 and 0.2 g/L) on the membrane performance and microbial community in GDM systems for primary municipal wastewater treatment. The results showed that dosing microplastics in the GDM systems led to 9–54% lower permeate flux than that in the control. This was attributed to more cake formation (up to 6.4-fold) with more deposition of extracellular polymeric substances (EPS, up to 1.5-fold) and divalent cations (up to 2.1-fold) in the presence of microplastics, especially with increasing microplastic amount or size. However, the dosed microplastics promoted formation of heterogeneous cake layers with more porous nature, possibly because microplastics created void space in the cake and also tended to bind with divalent cations to reduce EPS-divalent cations interactions. In the biofilm of the GDM systems, the presence of microplastics could lower the number of total species, but it greatly enhanced the abundance of certain dominant prokaryotes (Phenylobacterium haematophilum, Planctomycetota bacterium, and Flavobacteriales bacterium), eukaryotes (Stylonychia lemnae, Halteria grandinella, and Paramicrosporidium saccamoebae), and virus (phylum Nucleocytoviricota), as well as amino acid and lipid metabolic functions. Especially, the small-size microplastics at a higher dosed amount led to more variations of microbial community structure and microbial metabolic functions.

A New Methodological Approach to Study the Interaction of Humic Acids, Minerals and Polyvalent Cations in Soil

ABSTRACT A new methodological approach of humic acid (HA) extraction is applied to study soil samples with contrasting management regimes: natural vegetation (NV) and agricultural (A). This innovative approach involves a modification of the Swift’s method, wherein several steps HCl/HF are replaced by a single-step HCl/HF. This modification enabled us to investigate the ability of HA to retain inorganic constituents. The carbon content was significantly higher in soils under NV (19.8–27.3 g C kg−1) than under A (11.2–13.4 g C kg−1). The same pattern was observed for the HA content. The new methodology revealed that HA from NV soils had a much higher capacity to retain inorganics (ash contents in HA from 12.3–28.3%) than in A soils (ash content in HA from 1.6–2.6%). Similar results were found for Ca+Al+Fe contents in the HA (3.7–2.5 meq g−1 in HA from NV soils; 2.2–.9 meq g−1 in HA from A soils). Some differences were observed in IR spectra, mainly an intense band at around 1050 cm−1 of HA from NV that reflects the high ash content of the HA and its capacity of retaining inorganic material. Ca binding isotherms of HA also showed that the HA differed significantly in their ability to retain inorganic components when extracted. Humic acid from NV was more efficient in retaining metal ions and minerals than HA from A soils. All results point to a better contact between organic and inorganic matter in NV soils, and this contact contributes to the stabilization of organic matter.

Ion and Water Dynamics in the Transition from Dry to Wet Conditions in Salt-Doped PEG.

The influence of the water content on ion and water transport mechanisms in polymer membranes under low to moderate hydration conditions remains poorly understood. In this study, we combine ion and water diffusivity (PFG-NMR) measurements with atomistic molecular dynamics simulations to better understand transport processes in hydrated salt-doped poly(ethylene glycol). Above the water percolation threshold, the experimental and simulated diffusivities are in good agreement with the free volume transport models. At low hydration levels, unlike dry systems, ion diffusion cannot be described by polymer segmental dynamics alone. We rationalize such observations by the interplay between ion-water and ion-polymer solvation of cations and between ion-water and cation-anion interactions for anions. Further, we demonstrate that a two-state model combining ion-water solvation and free volume transport can describe water dynamics across the entire hydration range of interest. Our findings provide a more encompassing analysis of ion and water transport in hydrated polyelectrolytes, specifically in the low hydration regime.

Adsorption features of reduced aminated supports modified with glutaraldehyde: Understanding the heterofunctional features of these supports

Immobilization of enzymes on aminated supports using the glutaraldehyde chemistry may involve three different interactions, cationic, hydrophobic, and covalent interactions. To try to understand the impact this heterofunctionality, we study the physical adsorption of the beta-galactosidase from Aspergillus niger, on aminated supports (MANAE) and aminated supports with one (MANAE-GLU) or two molecules of glutaraldehyde (MANAE-GLU-GLU). To eliminate the chemical reactivity of the glutaraldehyde, the supports were reduced using sodium borohydride. After enzyme adsorption, the release of the enzyme from the supports using different NaCl concentrations, Triton X100, ionic detergents (SDS and CTAB), or different temperatures (4 °C to 55 °C) was studied. Using MANAE support, at 0.3 M NaCl almost all the immobilized enzyme was released. Using MANAE-GLU, 0.3 M, and 0.6 M NaCl similar results were obtained. However, incubation at 1 M or 2 M NaCl, many enzyme molecules were not released from the support. For the MANAE-GLU-GLU support, none of the tested concentrations of NaCl was sufficient to release all enzyme bound to the support. Only using high temperatures, 0.6 M NaCl, and 1 % CTAB or SDS, could the totality of the proteins be released from the support. The results shown in this paper confirm the heterofunctional character of aminated supports modified with glutaraldehyde.

New Local Composition Model for Correlating of the Molar Conductivity of Ionic Liquid-Solvent Systems over the Whole Concentration Range.

Considering that traditional electrolyte models are limited to use in the solvent-rich region, the development of new models to describe the molar conductivity (Λm) over the whole concentration range of ionic liquid (IL)-solvent systems is a meaningful study. Based on the idea of local composition and the law of independent ion migration, a new model is proposed in this study and used to successfully correlate the relationship between Λm and composition over the whole concentration range for 18 IL-solvent systems with satisfactory fitting accuracy. Meanwhile, the electrical conductivity (κ) of the systems is estimated using the calculated Λm. Moreover, the strength of anion-cation, anion-solvent, and cation-solvent interactions in the systems is explored by the obtained energy parameters, and the effect of the solvent on the interactions is investigated. The proposed model provides a new method to accurately describe the conductivity property of IL-solvent systems over the whole concentration range.

Assessment of the dynamic growth and potassium solubilization capability of three novel bacteria

Abstract. Bangun IH, Ketaren BR, Munar A, Sembiring P, Nurhajijah, Abdi A, Sitorus RS. 2024. Assessment of the dynamic growth and potassium solubilization capability of three novel bacteria. Biodiversitas 25: 177-185. Clay minerals are essential components that play a crucial role in soil cation exchangeable capacity and optimal plant growth. These components, including potassium (K), have the ability to bind with mineral crystals in the soil. Several studies have shown that K-solubilizing bacteria can facilitate the solubility of potassium, leading to optimal availability. However, the use of bacteria as biofertilizers is still limited due to challenges related to survival and growth patterns. To address these challenges, it is important to monitor the growth of the microbes and enhance their selection process to achieve effective utilization. Therefore, this study aimed to determine the bacterial growth dynamics and potential of Burkholderia paludis IHB_01, Burkholderia cepacia IHB_02, and Paraburkholderia phymatum IHB_03 in enhancing soil cation availability on clay minerals. The results showed a common initial adaptation phase among the 3 bacterial strains, followed by distinct exponential growth patterns. Burkholderia cepacia IHB_02 had the longest exponential growth phase, showing efficient resource utilization and extended growth. The results of soil cation enhancement by these bacteria showed that there were no major changes in measured parameters, such as total K, CEC, pH, and organic carbon. Furthermore, the variation in K exchange, organic carbon, and Na exchange provided insights into their unique interactions in the soil. The non-significant impact on potassium-related parameters in this study could be attributed to the presence of antagonistic cation interactions.

Fast Organic Cation Exchange in Colloidal Perovskite Quantum Dots toward Functional Optoelectronic Applications.

Colloidal quantum dots with lower surface ligand density are desired for preparing the active layer for photovoltaic, lighting, and other potential optoelectronic applications. In emerging perovskite quantum dots (PQDs), the diffusion of cations is thought to have a high energy barrier, relative to that of halide anions. Herein, we investigate the fast cross cation exchange approach in colloidal lead triiodide PQDs containing methylammonium (MA+) and formamidinium (FA+) organic cations, which exhibits a significantly lower exchange barrier than inorganic cesium (Cs+)-FA+ and Cs+-MA+ systems. First-principles calculations further suggest that the fast internal cation diffusion arises due to a lowering in structural distortions and the consequent decline in attractive cation-cation and cation-anion interactions in the presence of organic cation vacancies in mixed MA+-FA+ PQDs. Combining both experimental and theoretical evidence, we propose a vacancy-assisted exchange model to understand the impact of structural features and intermolecular interaction in PQDs with fewer surface ligands. Finally, for a realistic outcome, the as-prepared mixed-cation PQDs display better photostability and can be directly applied for one-step coated photovoltaic and photodetector devices, achieving a high photovoltaic efficiency of 15.05% using MA0.5FA0.5PbI3 PQDs and more precisely tunable detective spectral response from visible to near-infrared regions.

A Stimuli-Responsive Dual-Emitting Covalent Organic Framework Shows Selective Sensing of Highly Corrosive Acidic Media via Fluorescence Turn-On Signal with White Light Emission.

Luminescent covalent organic frameworks (LCOFs) have been employed as platforms for sensing analytes. Judicial incorporation of appropriate functional units inside the framework leads to the different electronic states in the presence of external stimuli, e.g., temperature, pH, etc. We report herein a new COF (TPEPy) as a solid-state acid sensor specific for the highly acidic environments that range from pH ∼0.5 to ∼3.0. This COF shows a protonation-induced reversible color change from bright yellow to deep red upon decreasing the pH from 3 to 0.5 and vice versa. No visual color change was, however, observed above pH 3.0. Photoluminescence (PL) studies show that the intrinsic emission peak of the TPEPy COF at 530 nm is shifted to 420 nm owing to the N-protonation of the imine nitrogen of COF within this pH range. Extensive studies demonstrate that the protonation behavior of the COF is counterion dependent. This was revealed when different acids, e.g., HCl, HNO3, HBr, and HI, were employed. The intensity of the proton-induced emission peak at 420 nm depends significantly upon the counterions with the order of HCl > HNO3 > HBr > HI. These anions interact with the protonated TPEPy COF by cation-anion and H-bonding interactions. Further, the pristine COF showed near white light emission at a particular pH of 2.5 (CIE coordinates 0.27, 0.32). From the PL spectrophotometric titrations, the deprotonation pKa was experimentally found to be 1.8 ± 0.02 for the TPEPy COF. The sensor reported herein is reversible, reusable, and regenerable and is useful for assessing pH fluctuations within a strongly acidic range via digital signaling.

Improving separation of CH4 and N2 by adsorption on zeolite Y Ion–Exchanged with ammonium Cations: An experimental and Grand–Canonical Monte Carlo (GCMC) simulation investigation

The separation of methane (CH4) from industrially–important nitrogen (N2)-rich vent streams such as those in liquefied natural gas processing plants is challenging. Pressure swing adsorption (PSA) is a promising, cost–effective solution in gas separation, especially for small–scale units. Further development and commercialisation of PSA–based technologies require access to low–cost, selective adsorbent materials. The current work investigates the improved separation of CH4 from N2 by TMA–Y zeolite which is obtained from the ion exchange treatment of Na–Y zeolite with the ammonium salt tetramethylammonium chloride (TMACl). TMA–Y is commercially called Ionic Liquidic Zeolite (ILZ), patented at The University of Western Australia, and has now been demonstrated on tonne–scale. In particular, we use a combination of experimental and molecular simulation techniques to provide insights into the high CH4–over–N2 selectivity of TMA–Y. For this, we obtain equilibrium isotherms of CH4 and N2 on Na–Y at different temperatures and pressures before and after ion exchange. The true selectivities of the zeolite samples are determined using the Ideal Adsorbed Solution Theory (IAST) and binary–gas grand–canonical Monte Carlo (GCMC) molecular simulations. From experiments and IAST calculations, we report an increase of >110% in the CH4/N2 selectivity of Na–Y after treatment with TMACl (from 2.2 to 4.7 at 5.0 MPa and 303.15 K for a mixture of 0.1 CH4+0.9 N2 mol.mol−1). GCMC molecular simulations provide a detailed picture of the molecular origins of this effect. Specifically, the introduction of TMA+ ions into the structure of Na–Y zeolite leads to a reduction of the available adsorption volume by more than 40% (from 0.30 to 0.17 cm3.g−1 with N2 as the probe molecule) for both adsorbing gas species (i.e. CH4 and N2). However, at the same time, this leads to stronger CH4–cation interactions due to the much higher affinity of TMA+ cations (5 kJ.mol−1) than extra–framework Na+ cations (1 kJ.mol−1) towards CH4. The overall effect of these two trends combined is the higher selectivity of the resulting TMA–Y zeolite for CH4. These molecular insights are useful in the systematic engineering of new materials with improved separation performance.

Influence of Divalent Cation Inhibition and Dissolved Organic Matter Enhancement on Phenol Oxidation Kinetics by Manganese Oxides.

Manganese oxides can oxidize organic compounds, such as phenols, and may potentially be used in passive water treatment applications. However, the impact of common water constituents, including cations and dissolved organic matter (DOM), on this reaction is poorly understood. For example, the presence of DOM can increase or decrease phenol oxidation rates with manganese oxides. Furthermore, the interactions of DOM and cations and their impact on the phenol oxidation rates have not been examined. Therefore, we investigated the oxidation kinetics of six phenolic contaminants with acid birnessite in ten whole water samples. The oxidation rate constants of 4-chlorophenol, 4-tert-octylphenol, 4-bromophenol, and phenol consistently decreased in all waters relative to buffered ultrapure water, whereas the oxidation rate of bisphenol A and triclosan increased by up to 260% in some waters. Linear regression analyses and targeted experiments demonstrated that the inhibition of phenol oxidation is largely determined by cations. Furthermore, quencher experiments indicated that radical-mediated interactions from oxidized DOM contributed to enhanced oxidation of bisphenol A. The variable changes between compounds and water samples demonstrate the challenge of accurately predicting contaminant transformation rates in environmentally relevant systems based on experiments conducted in the absence of natural water constituents.

Competitive Coordination Structure Regulation in Deep Eutectic Electrolyte for Stable Zinc Batteries.

Rechargeable zinc-based batteries are finding their niche in energy storage applications where cost, safety, scalability matter, yet they are plagued by rapid performance degradation due to the lack of suitable electrolytes to stabilize Zn anode. Herein, we report a competitive coordination structure to form unique quaternary hydrated eutectic electrolyte with ligand-cation-anion cluster. Unraveled by experiment and calculation results, the competing component can enter initial primary coordination shell of Zn2+ ion, partially substituting Lewis basic eutectic ligands and reinforcing cation-anion interaction. The hydration-deficient complexes induced between competing eutectic as hydrogen bond donor-accepter and water also broaden the electrochemical window and confine free water activity. The altered coordination further leads to robust hybrid organic-inorganic enriched solid electrolyte interphase, enabling passivated surface and suppressed dendrite growth. Noticeably, stable Zn plating/stripping for 8000 cycles with high Coulombic efficiencies of 99.6 % and long cycling life of 10000 cycles for Zn-organic batteries are obtained. Even under harsh conditions (small N/P ratio, low temperature), the profits brought by the competitive eutectic electrolyte are still very prominent. This design principle leveraged by eutectic electrolytes with competitive coordination offers a new approach to improve battery performance.